A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084798



Internal ID21994031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93695373..93695373hg38UCSC Ensembl
chr9:96457655..96457655hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084798
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer